Exocrine pancreatic dysfunction is common in hepatocyte nuclear factor 1β-associated renal disease and can be symptomatic

Author:

Clissold Rhian L12,Fulford Jon12,Hudson Michelle12,Shields Beverley M1,McDonald Timothy J1,Ellard Sian1,Hattersley Andrew T12,Bingham Coralie3

Affiliation:

1. Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK

2. National Institute for Health Research Exeter Clinical Research Facility, Royal Devon and Exeter National Health Service Foundation Trust, Exeter, UK

3. Exeter Kidney Unit, Royal Devon and Exeter National Health Service Foundation Trust, Exeter, UK

Funder

Medical Research Council Clinical Training

National Institute for Health Research Exeter Clinical Research Facility

National Institute for Health Research Senior Investigator

Wellcome Trust Senior Investigator

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Reference29 articles.

1. Expression of the vHNF1/HNF1β homeoprotein gene during mouse organogenesis;Coffinier;Mech Dev,1999

2. Prevalence of mutations in renal developmental genes in children with renal hypodysplasia: results of the ESCAPE study;Weber;J Am Soc Nephrol,2006

3. HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort;Thomas;Pediatr Nephrol,2011

4. Severe prenatal renal anomalies associated with mutations in HNF1B or PAX2 genes;Madariaga;Clin J Am Soc Nephrol,2013

5. HNF1B mutations associate with hypomagnesemia and renal magnesium wasting;Adalat;J Am Soc Nephrol,2009

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